材料科学
紫杉醇
体外
肽
体内
两亲性
细胞毒性
生物物理学
药物输送
癌细胞
胶束
癌症研究
组合化学
化学
阿霉素
作者
Yun Zheng,Pan Zhongwu,Xiaoxuan Zuo,Xiaojian Li,Fei Ge,Gui Lin
标识
DOI:10.1557/s43578-021-00132-6
摘要
Amphiphilic polypeptide P15 (YIGSRHHHLLLGFLG) was designed and synthesized for the encapsulation of paclitaxel to prepare targeted nano-microspheres (P15-PTX). The self-assembly behavior and drug-loading effect of P15-PTX in aqueous solution were investigated. The micelle-forming ability and in vitro antitumor activity of P15-PTX were also studied. The results showed that the mixing of P15 and PTX at an optimal ratio of 6:1 resulted in the formation of microspheres with regular rounded morphology, small particle size, high drug-loading rate, good drug release effect, high cell inhibition rate, enhanced antitumor activity, and a certain dose–response relationship with the P15-PTX concentration. At a P15-PTX concentration of 400 μg/mL, the proliferation inhibition rate of MCF-7 cells was 70%. The microsphere designed and prepared in this study is expected to provide a targeted drug delivery system with good application prospects for the treatment of tumor cells.
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